The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 589 (6%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mis labeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

6526–6550 of 9611

  • ModerateFDA (Devices)·Z-1544-2015·2015-05-06

    Integra Tuohy Needles Recalled for Incorrect Length Labeling

    Integra LifeSciences is recalling 90 Tuohy needles that were incorrectly labeled as 5 inches when they are actually 3.5 inches.

    Product
    Integra Long Epidural Steroid Injection Needle (Tuohy Needle), 18 Gauge x 5 inch Removable Wing, Metal Stylet, Calibrations (10BX), Catalogue No. PITRW1850. Used to administer steroid medication in the epidural space.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1560-2015·2015-05-06

    Bard Access Systems Recalls PowerLoc MAX Safety Winged Infusion Set

    Bard Access Systems is recalling 700 units of the PowerLoc MAX Safety Winged Infusion Set due to a potential incorrect Maximum Flow rate label on the packaging.

    Product
    PowerLoc MAX Safety Winged Infusion Set, Product Code 0132215 The PowerLoc MAX Safety Winged Infusion Set is intended for use in the administration of fluids and drugs, as well as blood sampling through surgically implanted vascular ports. The PowerLoc MAX SWIS is also indicat
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1550-2015·2015-05-06

    Fresenius 2008T Hemodialysis Machines Recalled for Acetate Display Error

    Fresenius Medical Care is recalling 2008T hemodialysis machines because the Select Concentrate screen incorrectly displays the GranuFlo acetate value as 4mEq/l instead of 8mEq/l.

    Product
    2008 Series Hemodialysis Machines: 2008T with the following product code and description: 190395 2008K at Home System - 1st Gen. -¿ Canada; 190828 2008K at Home System - 2nd Gen - U.S.; 190904 2008K at Home System w/ Bibag; 190828 2008KatHOME HEMODIALYSIS SYSTEM; 190395 2008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V258000·2015-05-01

    Starcraft RV Recalls 2016 Travel Trailers with Incorrect Tire Labels

    Starcraft RV is recalling 36 model year 2016 Launch and AR-One travel trailers because Federal Certification Labels may list the wrong tire size.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE, LAUNCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·072-2015·2015-04-30

    Ohanyan's Recalls Sausage Products Due to Undeclared Soy Allergen

    Ohanyan's Inc. is recalling approximately 159,291 pounds of dried beef sausage products because they contain undeclared soy lecithin, a known allergen.

    Product
    Ohanyan's Inc. — Ohanyan's Bastirma and Soujouk, Co. Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2020-2015·2015-04-29

    La Guadalupana Vegan Tamales Recalled for Undeclared Egg White Powder

    La Guadalupana Wholesale Co Inc is recalling Salsa Verde Vegan Tamales because they may contain undeclared egg white powder. The product was distributed in Indiana, Illinois, and Canada.

    Product
    La Guadalupana Salsa Verde Vegan Tamales are packed in a bulk plastic bag inside of a corrugated box and are stored frozen or refrigerated until cooked for consumption.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2025-2015·2015-04-29

    Giant Eagle Recalls Turkey and Swiss Sandwiches for Undeclared Egg Allergen

    Giant Eagle is recalling select GetGo Turkey and Swiss sandwiches because they contain egg, which is not listed on the label.

    Product
    GetGo GNG 7 Inch Turkey N Swiss Sell By: (up to and including) 04/02/15 Net Wt: 6.0 Oz. Contains: Milk, Soy, Wheat; UPC: 65567 20399 GetGo from Giant Eagle Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238 Sandwich is wrapped in plastic.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2024-2015·2015-04-29

    Giant Eagle Recalls Italian Subs for Undeclared Egg Allergen

    Giant Eagle is recalling 4,671 units of GetGo 7-inch Italian subs sold in Maryland, Ohio, Pennsylvania, and West Virginia due to an undeclared egg allergen.

    Product
    GetGo GNG 7 Inch Italian Sub Sell By: (up to and including) 04/02/15 Net Wt: 6.0 Oz. Contains: Soy, Milk, Wheat UPC: 25567 20399 GetGo from Giant Eagle Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238 Sandwich is wrapped in plastic.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1951-2015·2015-04-29

    Giant Eagle Recalls GetGo Strawberry Yogurt Parfait for Undeclared Soy

    Giant Eagle is recalling GetGo Strawberry Yogurt Parfait because the label failed to declare soy, a major allergen, present in the granola ingredient.

    Product
    GetGo Giant Eagle Strawberry Yogurt Parfait Sell By: (up to and including) 3/24/2015 Distributed by: Giant Eagle, Inc., Pittsburgh, PA 15238 Contains: Milk, Wheat, Almonds Net Wt: 10 oz.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1512-2015·2015-04-29

    Xpress System Pedicle Screw Assembly Recalled for Incorrect Laser Marking

    X Spine Systems Inc is recalling 14 units of Xpress System Pedicle Screw Assemblies because the laser marking on the yoke incorrectly states 7.5 x 55mm instead of 5.5 x 55mm.

    Product
    Xpress System Pedicle Screw Assembly, 5.5 x 55mm. An internal fixation device for spinal surgery consisting of rods, pedicle screw assemblies (screw, cap, yoke) and cross bar connector assemblies.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1479-2015·2015-04-29

    SpineFrontier Recalls MISquito Pedicle Screw System Surgical Technique Document

    SpineFrontier is recalling the MISquito Pedicle Screw System Surgical Technique document because it does not adequately convey the intended use of the Rod Caliper.

    Product
    SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique; Part Number: DOC80023. The Rod Caliper is a manual surgical instrument that may be used as part of the PedFuse Pedicle Screw System and its MISquito components during percutaneous, minimally invasive
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1459-2015·2015-04-29

    Exactech Recalls Equinoxe 44mm Short Humeral Head Shoulder Implants

    Exactech, Inc. is recalling 112 Equinoxe 44mm Short Humeral Head shoulder implant components because incorrect outer and inner labeling may misidentify the device size.

    Product
    Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic shoulder implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1481-2015·2015-04-29

    Catheter Research Recalls Mislabeled HSG Trays and Catheters

    Catheter Research, Inc. is recalling 880 HSG trays and catheters because the flexible and shapeable catheters were mislabeled on the packaging.

    Product
    HSG Trays/HS 5F Catheter Combo; HSG Procedure Tray+ Shapeable 5F HSG catheter. For hysterosonography and hysterosalpingography, gynecological use.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1516-2015·2015-04-29

    PhotoMedex Recalls Iamin Medical Devices Due to Inconsistent Labeling

    PhotoMedex, Inc. is recalling Iamin Moist Dressings and Hydrating Gel because their labeling does not match the intended uses approved by the FDA.

    Product
    Iamin Moist Dressing and the Iamin Hydrating Gel: intended to cover a wound or burn on the skin, provide a moist wound environment and protect against abrasion, friction, desiccation and contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·069-2015·2015-04-24

    Alpine Sausage Kitchen Recalls Beef and Pork Sausages for Undeclared Soy

    Alpine Sausage Kitchen is recalling approximately 3,350 pounds of beef and pork sausage products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Alpine Sausage Kitchen Recalls Beef And Pork Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1960-2015·2015-04-22

    Trader Joe's Pita Bread Recalled for Undeclared Soy Allergen

    Middle East Bakery is recalling Trader Joe's Pocketful of Fiber Pita Bread because it may contain undeclared soy.

    Product
    Trader Joe's Pocketful of Fiber Pita Bread, UPC 00945097
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1945-2015·2015-04-22

    ReNew Life Formulas Recalls Multi-Plus Vitamins Due to Gluten Mislabeling

    ReNew Life Formulas is recalling PureLife Naturals Adult Multi-Plus vitamins because labels claim 'no wheat' and 'no gluten' but the products contain gluten or wheat.

    Product
    PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle
    Category
    Food
    Distribution
    51 states
  • HighFDA (Food)·F-1946-2015·2015-04-22

    PureLife Naturals Multi-Action Immunity Recalled for Gluten Mislabeling

    ReNew Life Formulas is recalling PureLife Naturals Multi-Action Immunity supplements because labels claim 'no wheat' and 'no gluten' but the products contain gluten or wheat-related allergens.

    Product
    PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle
    Category
    Food
    Distribution
    51 states
  • ModerateFDA (Devices)·Z-1446-2015·2015-04-22

    Biomet Recalls Low Profile Non-Locking Screws Due to Anodizing Error

    Biomet is recalling 45 Low Profile Non-Locking Screws because they were anodized green instead of the required gold color.

    Product
    LOW PROFILE NON-LOCK SCREW; 2.7mm x 22 mm; REF 131227222; LOT RM105E. Provides the orthopaedic surgeon a means of bone fixation and helps generally in the management of fractures and reconstructive surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1444-2015·2015-04-22

    Hardy Diagnostics Recalls HardyCHROM SS Agar Due to Color Development Issue

    Hardy Diagnostics is recalling HardyCHROM SS Agar (Lot 15037) due to a report of possible lack of color development in Shigella organisms.

    Product
    Hardy Diagnostics cat no. G327 HardyCHROM SS Agar (HardyCHROM Salmonella Shigella) Cat no: G327 Container type: 15x100mm monoplate Packaged: 10 plates/sleeve Storage: 2 to 8 degrees C. on receipt in dark A selective chromogenic medium for the primary screening isolati
    Category
    Medical Device
    Distribution
    6 states
  • LowFDA (Drugs)·D-0489-2015·2015-04-22

    Cardinal Health Recalls Potassium Chloride Tablets Due to Incorrect Package Insert

    Cardinal Health is recalling specific lots of potassium chloride extended-release tablets because they were packaged with the wrong package insert.

    Product
    Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated shipper, Rx only, Manufactured by Upsher-Smith Laboratories, Inc. Minneapolis, MN 55447 for Sandoz, Inc., Princeton, NJ 08540 Repackaged by Cardinal Health Zanesvil
    Category
    Drug
    Distribution
    1 state
  • HighNHTSA·15V237000·2015-04-21

    Coachmen Freelander and Leprechaun Recalled for Incorrect Weight Labels

    Forest River is recalling 2015-2016 Coachmen Freelander and 2015 Leprechaun vehicles because incorrect weight labels may lead to overloading and increased crash risk.

    Product
    COACHMEN — COACHMEN FREELANDER, LEPRECHAUN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·065-2015·2015-04-20

    Michigan Brand Recalls Smoked Turkey and Beef for Labeling Error

    Michigan Brand, Inc. is recalling approximately 737 pounds of smoked turkey and beef products because the labels failed to list sodium nitrite as an ingredient.

    Product
    Michigan Brand, Inc. — Recall Notification Report 065-2015 (Turkey and Beef)
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·063-2015·2015-04-17

    Royal Frozen Food Recalls Beef and Chicken Blintzes Due to Undeclared Milk

    Royal Frozen Food is recalling beef and chicken blintzes because they contain undeclared milk, a known allergen. The products were distributed in California and Nevada.

    Product
    Royal Frozen Food — Royal Frozen Food Recalls Beef and Chicken Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1879-2015·2015-04-15

    Texamerican Cumin Recalled Due to Undeclared Peanut Allergen

    Texamerican Food Blending is recalling 5 lb. bags of Cumin because two lots of ingredients were contaminated with peanut allergen, which is not listed on the label.

    Product
    Texamerican Cumin 5 lbs. Item Number: ARCH075-05
    Category
    Food
    Distribution
    4 states